A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997614



Internal ID19157150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53220560..53284465hg38UCSC Ensembl
Innerchr4:54086727..54150632hg19UCSC Ensembl
Innerchr4:53781484..53845389hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3863906
hg1963906
hg1863906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625259
Samples
Known GenesSCFD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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